Acetylene-terminated ethylene oxide tetrahydrofuran copolyether containing carbamic acid ester units and synthesis method thereof

A technology of alkynyl-terminated oxirane tetrahydrofuran copolyether and hydroxyl-terminated oxirane tetrahydrofuran copolyether, which is applied in the field of alkynyl-terminated oxirane tetrahydrofuran copolyether and its synthesis, and can solve the problem of polytriazole fracture elongation Low-level problems, to achieve the effect of improving mechanical properties

Inactive Publication Date: 2017-02-01
XIAN MODERN CHEM RES INST
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

The polytriazole elastome...

Method used

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  • Acetylene-terminated ethylene oxide tetrahydrofuran copolyether containing carbamic acid ester units and synthesis method thereof
  • Acetylene-terminated ethylene oxide tetrahydrofuran copolyether containing carbamic acid ester units and synthesis method thereof
  • Acetylene-terminated ethylene oxide tetrahydrofuran copolyether containing carbamic acid ester units and synthesis method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0017] (1) Synthesis of propargyl (3-isocyanato-4-methyl) phenyl carbamate

[0018] Under nitrogen protection, 5.6 g (0.1 mol) of propynyl alcohol was added dropwise to a mixture of 52.2 g (0.3 mol) of toluene-2,4-diisocyanate and 100 mL of toluene, and the temperature was kept at 40° C. during the dropwise addition. After the dropwise addition, react at 60°C for 6h to end the reaction. After cooling down, a solid was precipitated, filtered and dried to obtain 14 g of a white solid with a yield of 60.9%.

[0019] Characterization data:

[0020] 1 H NMR (DMSO-d 6 ,500MHz): δ=9.90(s,1H),7.31(s,1H),7.19(m,2H),4.76(d,2H,J=2.0Hz),3.56(t,1H,J=2.0Hz) ,2.23(s,3H); 13 C NMR (DMSO-d 6 ,125MHz): δ=153.0,138.2,132.3,131.3,127.2,124.6,116.4,114.9,79.3,78.0,52.5,17.6.

[0021] IR(KBr,cm -1 ):ν=3331, 3294, 2281, 2124, 1714, 1623, 1553, 1516, 1388, 1314, 1283, 1227, 1075, 916;

[0022] Elemental Analysis: C 12 h 10 N 2 o 3 , theoretical value C 62.6, H 4.38, N 12.17; calculated v...

Embodiment 2

[0031] (1) Synthesis of propargyl (3-isocyanato-4-methyl) phenyl carbamate

[0032] Under nitrogen protection, 5.6 g (0.1 mol) propynyl alcohol was added dropwise to a mixture of 69.6 g (0.4 mol) toluene-2,4-diisocyanate and 100 mL toluene, and the temperature was kept at 50° C. during the dropwise addition. After the dropwise addition, react at 60°C for 6h to end the reaction. After cooling down, a solid was precipitated, filtered and dried to obtain 14.2 g of a white solid, with a yield of 62.0%.

[0033] (2) Synthesis of tetrahydrofuran copolyether containing carbamate unit-terminated alkynyl oxirane tetrahydrofuran

[0034] Under nitrogen protection, 15.3g (66.6mmol) propargyl (3-isocyanato-4-methyl) phenyl carbamate, 100g hydroxyl-terminated oxirane tetrahydrofuran block copolyether (66.6mmol OH) and Add 500mL of dry toluene to the reaction flask. After stirring at 70°C for 24 hours, the reaction was terminated, and the toluene was concentrated to drive off to obtain 1...

Embodiment 3

[0036] (1) Synthesis of propargyl (3-isocyanato-4-methyl) phenyl carbamate

[0037] Under nitrogen protection, 5.6 g (0.1 mol) propynyl alcohol was added dropwise to a mixture of 87 g (0.5 mol) toluene-2,4-diisocyanate and 100 mL toluene, and the temperature was kept at 50° C. during the dropwise addition. After the dropwise addition, react at 70° C. for 5 h to end the reaction. After cooling down, a solid was precipitated, filtered and dried to obtain 15.6 g of a white solid with a yield of 68.1%.

[0038] (2) Synthesis of tetrahydrofuran copolyether containing carbamate unit-terminated alkynyl oxirane tetrahydrofuran

[0039] Under nitrogen protection, 1.15g (5mmol) propargyl (3-isocyanato-4-methyl) phenyl carbamate, 11.5g hydroxyl-terminated oxirane tetrahydrofuran random copolymer ether (5mmol OH) and 100mL Add dry toluene to the reaction flask. After stirring at 60°C for 24 hours, the reaction was terminated, and the toluene was removed by concentration to obtain 11.5 ...

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Abstract

The invention discloses an acetylene-terminated ethylene oxide tetrahydrofuran copolyether containing carbamic acid ester units. The structural formula is shown in the picture I. A synthesis process includes the steps that 1, propargyl alcohol reacts with an excessive amount of toluene-2,4-diisocyanate, and then propargyl (3-isocyanate group-4-methyl) phenyl carbamate is obtained; 2, propargyl (3-isocyanate group-4-methyl) phenyl carbamate and terminal hydroxyl ethylene oxide tetrahydrofuran copolyether generate the acetylene-terminated ethylene oxide tetrahydrofuran copolyether containing the carbamic acid ester units through an additive reaction. The acetylene-terminated ethylene oxide tetrahydrofuran copolyether containing the carbamic acid ester units has a specific chain structure, is free of side reactions, and is applied to a polytriazole elastomer so that the polytriazole elastomer can have excellent mechanical properties.

Description

technical field [0001] The invention relates to an alkynyl-terminated oxirane tetrahydrofuran copolyether containing carbamate units and a synthesis method thereof. The compound can be used as a binder for composite solid propellants and belongs to the technical field of polymer materials. Background technique [0002] Binder is an important component of solid propellant. It acts as a skeleton and matrix to bind oxidizer, metal aluminum powder, plasticizer and other additive components together, so that the propellant formula has certain geometric shape and mechanical properties. Hydroxyl-terminated polybutadiene (HTPB) propellants and hydroxyl-terminated polyether (HTPE) propellants, which are widely used in weaponry at present, are both cured by hydroxyl-terminated prepolymers and isocyanates at a certain temperature to form polyurethane elastomers. The reaction system is sensitive to moisture, and the moisture in the environment and raw materials will cause a series of si...

Claims

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Application Information

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IPC IPC(8): C08G65/333C08G73/08
CPCC08G65/33358C08G65/33396C08G73/08C08G2650/04
Inventor 李辉赵凤起王伯周李祥志廉鹏
Owner XIAN MODERN CHEM RES INST
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